Canonical Allele Identifier: CA346075861
Gene: ASXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742520T>C , CM000664.2:g.25742520T>C GRCh38
NC_000002.11:g.25965389T>C , CM000664.1:g.25965389T>C GRCh37
NC_000002.10:g.25818893T>C NCBI36
NG_052995.1:g.140997A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.3814A>G ENSP00000337250.5:p.Met1272Val
ENST00000435504.9:c.3817A>G MANE Select ENSP00000391447.3:p.Met1273Val
ENST00000336112.8:c.3733A>G ENSP00000337250.4:p.Met1245Val
ENST00000404843.5:c.2266A>G ENSP00000383920.1:p.Met756Val
ENST00000435504.8:c.3817A>G ENSP00000391447.3:p.Met1273Val
NM_018263.4:c.3817A>G NP_060733.4:p.Met1273Val
XM_006712039.2:c.3451A>G XP_006712102.1:p.Met1151Val
XM_006712040.1:c.3037A>G XP_006712103.1:p.Met1013Val
XM_011532950.1:c.3814A>G XP_011531252.1:p.Met1272Val
XM_011532951.1:c.3643A>G XP_011531253.1:p.Met1215Val
NM_018263.5:c.3817A>G NP_060733.4:p.Met1273Val
XM_006712039.3:c.3451A>G XP_006712102.1:p.Met1151Val
XM_006712040.2:c.3037A>G XP_006712103.1:p.Met1013Val
XM_011532950.3:c.3814A>G XP_011531252.1:p.Met1272Val
XM_011532951.2:c.3643A>G XP_011531253.1:p.Met1215Val
XM_017004430.1:c.3037A>G XP_016859919.1:p.Met1013Val
XM_024452974.1:c.3997A>G XP_024308742.1:p.Met1333Val
NM_001369346.1:c.3643A>G NP_001356275.1:p.Met1215Val
NM_001369347.1:c.3037A>G NP_001356276.1:p.Met1013Val
NM_018263.6:c.3817A>G MANE Select NP_060733.4:p.Met1273Val